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"DGH" Keratoscope (Non-Sterile) - Taiwan Registration 91c4a39e81030c3999a2eefb445bdff7

Access comprehensive regulatory information for "DGH" Keratoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91c4a39e81030c3999a2eefb445bdff7 and manufactured by DGH Technology Inc.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DGH Technology Inc., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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91c4a39e81030c3999a2eefb445bdff7
Registration Details
Taiwan FDA Registration: 91c4a39e81030c3999a2eefb445bdff7
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Device Details

"DGH" Keratoscope (Non-Sterile)
TW: "่ฟชๅฑ…ๆ›ฒ" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

91c4a39e81030c3999a2eefb445bdff7

Ministry of Health Medical Device Import No. 017752

DHA09401775209

Company Information

United States

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Apr 24, 2017

Apr 24, 2022

Cancellation Information

Logged out

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